Canonical Allele Identifier: CA362558051
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610531-C-A
MyVariant Identifiers: chr6:g.1610766C>A (hg19) chr6:g.1610531C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610531C>A , CM000668.2:g.1610531C>A GRCh38
NC_000006.11:g.1610766C>A , CM000668.1:g.1610766C>A GRCh37
NC_000006.10:g.1555765C>A NCBI36
NG_009368.1:g.5086C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.86C>A MANE Select ENSP00000493906.1:p.Ala29Glu
ENST00000380874.3:c.86C>A ENSP00000370256.2:p.Ala29Glu
NM_001453.2:c.86C>A NP_001444.2:p.Ala29Glu
NM_001453.3:c.86C>A MANE Select NP_001444.2:p.Ala29Glu
Search 100 bp 5'
Search 100 bp 3'